Understanding sickle cell disease: causes, symptoms, and treatment options

C Elendu, DC Amaechi, CE Alakwe-Ojimba… - Medicine, 2023 - journals.lww.com
Sickle cell disease (SCD) is a hereditary blood disorder characterized by the production of
abnormal hemoglobin molecules that cause red blood cells to take on a crescent or sickle …

Current status of newborn screening worldwide: 2015

BL Therrell, CD Padilla, JG Loeber, I Kneisser… - Seminars in …, 2015 - Elsevier
Newborn screening describes various tests that can occur during the first few hours or days
of a newborn's life and have the potential for preventing severe health problems, including …

Sickle cell disease: advances in treatment

RV Gardner - Ochsner journal, 2018 - ochsnerjournal.org
Background: Sickle cell disease causes significant morbidity and mortality and affects the
economic and healthcare status of many countries. Yet historically, the disease has not had …

Role of epigenetics in developmental biology and transgenerational inheritance

MK Skinner - Birth Defects Research Part C: Embryo Today …, 2011 - Wiley Online Library
The molecular mechanisms involved in developmental biology and cellular differentiation
have traditionally been considered to be primarily genetic. Environmental factors that …

Genotypic and phenotypic composition of sickle cell disease in the Arab population-a systematic review

F Ata, A Rahhal, L Malkawi, P Iqbal… - Pharmacogenomics …, 2023 - Taylor & Francis
Sickle cell disease (SCD) is a genetic disease influenced by ethnicity and regional
differences in its clinical course. Recent advances in the management of SCD with newer …

Distribution of hemoglobinopathy disorders in Saudi Arabia based on data from the premarital screening and genetic counseling program, 2011–2015

ES Alsaeed, GN Farhat, AM Assiri, Z Memish… - Journal of epidemiology …, 2017 - Springer
The prevalence rates of β-thalassemia (β-thal) and Sickle Cell Disease (SCD) in Saudi
Arabia are considered one of the highest compared to surrounding countries in the Middle …

Consanguinity and genetic diseases in North Africa and immigrants to Europe

WA Anwar, M Khyatti, K Hemminki - The European Journal of …, 2014 - academic.oup.com
Endemic diseases are caused by environmental and genetic factors. While in this special
issue several chapters deal with environmental factors, including infections, the present …

[HTML][HTML] Epidemiology and characteristics of sickle cell patients admitted to hospitals in Jazan region, Saudi Arabia

AA Hazzazi, MH Ageeli, AM Alfaqih… - Journal of Applied …, 2020 - journals.lww.com
OBJECTIVES: This study aimed to describe the epidemiology and characteristics of sickle
cell patients admitted to hospitals in Jazan region. MATERIALS AND METHODS: A cross …

Assessment of perceptions and predictors towards consanguinity: a cross-sectional study from Palestine

M Ghanim, R Mosleh, A Hamdan, J Amer… - Journal of …, 2023 - Taylor & Francis
Background/Aim Consanguinity represents a biological relationship between two
individuals. In clinical genetics, it specifically refers to the marriage between individuals who …

Quality of life among caregivers of sickle cell disease patients: a cross sectional study

BM Madani, R Al Raddadi, S Al Jaouni, M Omer… - Health and quality of life …, 2018 - Springer
Purpose To assess the quality of life (QoL) of caregivers of children with sickle cell disease
(SCD) and to determine the risk factors associated with poor QoL. Method A cross sectional …